Medical Writer Salary at Cherry Gmbh BETA

Job Title: Medical Writer – Promotional Materials (Remote, Spain) Are you a talented Medical Writer with a passion for crafting compelling, scientifically accurate promotional content? Join a leading Medical Communications agency and help shape impactful materials for top healthcare and pharmaceutical clients. About the Role As a Medical Writer, you’ll focus on developing high-quality promotional materials across various channels, including sales aids, digital content, and marketing campaigns. You’ll work closely with cross-functional teams to ensure content is engaging, compliant, and aligned with brand strategies. Key Responsibilities Develop scientifically rigorous promotional materials for pharmaceutical and healthcare brands Adapt complex medical information into clear, engaging content for HCPs and patients Collaborate with internal teams (designers, editors, strategists) and external stakeholders Ensure all materials comply with industry regulations and guidelines (e.g., ABPI, E

Clinical Project Manager (Medical Writer) 8-month contract Onsite in Lake Forest, IL Job Summary: Our medical device client is seeking a Clinical Project Manager to support their IVDR remediation program by ensuring compliance in a timely manner. This role will involve data generation, literature searches, medical writing, and clinical study execution to support both on-market and new products requiring IVDR compliance. The ideal candidate will have experience in clinical research, medical writing, literature review protocols, and study execution with proficiency in Microsoft Word for document tracking and formatting. Key Responsibilities: Conduct literature searches, data collation, and dissemination to generate clinical performance reports for IVDR remediation. Develop literature search protocols and interpret/select relevant scientific literature. Write, review, and update clinical performance reports annually. Support clinical study start-up and execution for IVDR compliance, inclu

EPM is partnered with an innovative global biopharmaceutical company that is looking for a Senior Medical Writer to join their US team in the NJ/NY area. Key responsibilities: Creating clinical and regulatory documents including protocols, CSRs, CSPs, IBs, ICFs, CTDs, RMPs, PIPs, INDs, NSAs, BLAs, MAAs and additional briefing documents for various regulatory authorities like FDA, EMA, ICH, GCP, etc Developing clinical trial protocols and development plans Working cross-functionally with various teams like clinical, regulatory, and medical affairs Participating in internal and external meetings surrounding strategy, industry trends, evolving guidelines, and timelines A strong candidate for this role will bring: A PhD, PharmD, MD, or MSc A minimum of 3 years of direct medical writing experience in the biotech and/or pharmaceutical industry Prior experience with the above deliverables, documents, and submissions Experience working across various phases I-IV is a huge plus Experience in ne

Title: Clinical Medical Writer (IVDR/Medical Device) Duration: 9 months Location: Lake Forest, IL 60045 (Hybrid) Starting Rate: $45/hr One candidate will be recruited to work in Lake Forest, Chicago, and two candidates will be recruited to work in Europe. The US candidate is sought to fill one of the following positions: 1) Medical Writing: Additional clinical resource is required to support the ongoing IVDR remediation program, to ensure IVDR compliance in a timely manner. The Contingent Worker will support data generation through literature searches and data collation and dissemination. This will be in support of on-market products going through IVDR remediation. It is expected that the Contingent Worker will generate the initial clinical performance report, which then will be updated on an annual basis. The candidate will be skilled in medical writing, developing literature search protocols, and interpreting and selecting relevant scientific literature. Proficiency in Microsoft Word

TFS HealthScience is a leading global, mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full service-capabilities, resourcing and functional service (FSP) solutions. Scientific Communications Medical Writer About This Role The Medical Writer will support the development and maintenance of global medical information content, including writing and formatting, documentation, reporting and metrics on global Medical Information activities. The Medical Writer will work under the guidance of the Scientific Communications Manager in regard to content and timelines and adhere to defined client standards as well as safeguard that processes and system standards are followed. Key Responsibilities Production of new global standard scientific response content (gSSRC) as defined by the Scientific Communications Manager and in accordance with the client Medical Inform

Type of Requisition: Regular Clearance Level Must Currently Possess: None Clearance Level Must Be Able to Obtain: None Public Trust/Other Required: NACI (T1) Job Family: Technical Documentation Job Qualifications: Skills: Electronic Common Technical Document (eCTD), Government Affairs, Regulatory Writing Certifications: None Experience: 5 + years of related experience US Citizenship Required: Yes Job Description: GDIT's Military Health team is hiring a Medical Writer to support the Office of Regulated Activities (ORA) under the DoD (Dept. of Army) located at Ft. Detrick in Frederick, Maryland. The Office of Regulated Activities (ORA) is a multidisciplinary team of regulatory affairs, compliance, and clinical support professionals dedicated to supporting the USAMRDC mission of developing Food and Drug Administration regulated medical products for the Warfighter. The ORA provides full-service, oversight, and consultation for regulatory, clinical, non-clinical, manufacturing, data managem

Position Overview: This position supports the Clinical Development, Clinical Operations and Regulatory Affairs teams in writing and coordinating the writing and review of technical documents. Key Responsibilities: The Senior Medical Writer is responsible for the development and management of medical writing deliverables in support of key functions including Clinical Development, Clinical Operations, and Regulatory Affairs. The specific responsibilities of this role include, but are not limited to: Serve as the primary writer for a range of medical writing projects including the design, planning, and preparation of documents supporting clinical development (e.g., study protocols, study reports, investigator brochures, etc.), regulatory activities (e.g., briefing materials, clinical modules, etc.), and manuscript preparation. Ensure that documents are high-quality in terms of scientific content, organization, clarity, accuracy, format, consistency, and adherence to relevant internal and

Job title: Clinical Evaluations Specialist – Regulatory Documentation Location: Johns Creek, GA (onsite) Duration: 6 months (possible extension) Job Description: The Clinical Evaluations Specialist is responsible for managing regulatory documentation related to clinical evaluations, particularly for Medical Device Regulation (MDR) remediation and Post Production Risk Reviews (PPRRs). This role requires strong expertise in clinical literature reviews, regulatory writing, and post-market surveillance activities to support the life cycle management of medical devices. The specialist will serve as a primary point of contact for clinical project leads and collaborate closely with cross-functional teams, including Regulatory Affairs, Quality Assurance, and Clinical Development. Key Responsibilities: Regulatory Documentation & Clinical Evaluation: Author, revise, and update clinical documents for MDR remediation and PPRRs. Conduct systematic literature reviews and clinical data appraisals in